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人类前体信使核糖核酸3'加工复合体的分子结构

Molecular architecture of the human pre-mRNA 3' processing complex.

作者信息

Shi Yongsheng, Di Giammartino Dafne Campigli, Taylor Derek, Sarkeshik Ali, Rice William J, Yates John R, Frank Joachim, Manley James L

机构信息

Department of Biological Sciences, Columbia University, New York, NY 10027, USA.

出版信息

Mol Cell. 2009 Feb 13;33(3):365-76. doi: 10.1016/j.molcel.2008.12.028.

Abstract

Pre-mRNA 3' end formation is an essential step in eukaryotic gene expression. Over half of human genes produce alternatively polyadenylated mRNAs, suggesting that regulated polyadenylation is an important mechanism for posttranscriptional gene control. Although a number of mammalian mRNA 3' processing factors have been identified, the full protein composition of the 3' processing machinery has not been determined, and its structure is unknown. Here we report the purification and subsequent proteomic and structural characterization of human mRNA 3' processing complexes. Remarkably, the purified 3' processing complex contains approximately 85 proteins, including known and new core 3' processing factors and over 50 proteins that may mediate crosstalk with other processes. Electron microscopic analyses show that the core 3' processing complex has a distinct "kidney" shape and is approximately 250 A in length. Together, our data has revealed the complexity and molecular architecture of the pre-mRNA 3' processing complex.

摘要

前体mRNA 3'末端形成是真核基因表达中的一个关键步骤。超过半数的人类基因会产生可变聚腺苷酸化的mRNA,这表明受调控的聚腺苷酸化是转录后基因调控的一个重要机制。虽然已经鉴定出许多哺乳动物mRNA 3'加工因子,但3'加工机制的完整蛋白质组成尚未确定,其结构也未知。在此,我们报告了人类mRNA 3'加工复合物的纯化及其后续的蛋白质组学和结构表征。值得注意的是,纯化后的3'加工复合物包含约85种蛋白质,包括已知和新发现的核心3'加工因子以及50多种可能介导与其他过程相互作用的蛋白质。电子显微镜分析表明,核心3'加工复合物具有独特的“肾形”,长度约为250埃。我们的数据共同揭示了前体mRNA 3'加工复合物的复杂性和分子结构。

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